A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv878n145



Internal ID22813894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:48482589..48495288hg38UCSC Ensembl
chr4:48484606..48497305hg19UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3812700
hg1912700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116213, nsv3110529, nsv3112245, nsv3118277
Samplessample404, sample81, sample300, sample378, sample397
Known GenesSLC10A4, ZAR1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv878n145
Frequency
Sample Size467
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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